Results 21 to 30 of about 101,774 (257)

Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene [PDF]

Journal of Integrative Neuroscience, 2020
Autosomal recessive cerebellar ataxias comprise many types of diseases. The most frequent autosomal recessive cerebellar ataxias are Friedreich ataxia, but other types are relatively rare.
Haruo Shimazaki, Junya Kobayashi, Ryo Sugaya, Imaharu Nakano, Shigeru Fujimoto
doaj   +1 more source

Speech disorders in cerebellar disease [PDF]

Annals of Neurology, 1978
AbstractThe areas of cerebellar damage most commonly associated with dysarthria were sought by reviewing the clinical, radiographic, surgical, and autopsy findings in patients with nondegenerative cerebellar disease. Case histories on 162 patients with focal cerebellar lesions were reviewed.
Lechtenberg, Richard, Gilman, Sid
openaire   +3 more sources

Fractal dimension and variant anatomy of the white matter of the human cerebellar hemisperes

Journal of Education, Health and Sport, 2017
Introduction. Morphological changes of the cerebellar lobules are found in many congenital and acquired diseases of the cerebellum, but the information on the normal structure of the cerebellar lobules do not take into account the peculiarities of ...
N. I. Maryenko, O. Yu. Stepanenko
doaj   +3 more sources

Neurophysiology of cerebellar ataxias and gait disorders

Clinical Neurophysiology Practice, 2023
There are numerous forms of cerebellar disorders from sporadic to genetic diseases. The aim of this chapter is to provide an overview of the advances and emerging techniques during these last 2 decades in the neurophysiological tests useful in cerebellar
Mario Manto, Mariano Serrao, Stefano Filippo Castiglia, Dagmar Timmann, Elinor Tzvi-Minker, Ming-Kai Pan, Sheng-Han Kuo, Yoshikazu Ugawa   +7 more
doaj   +1 more source

Neuroradiological Findings in the Spinocerebellar Ataxias

Tremor and Other Hyperkinetic Movements, 2019
Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseases characterized by cerebellar ataxia.
Alex Tiburtino Meira, Walter Oleschko Arruda, Sergio Eiji Ono, Arnolfo de Carvalho Neto, Salmo Raskin, Carlos Henrique F. Camargo, Hélio Afonso G. Teive   +6 more
doaj   +1 more source

Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxia

Frontiers in Systems Neuroscience, 2023
The cerebellum plays a major role in balance, motor control and sensorimotor integration, but also in cognition, language, and emotional regulation.
Maurizio Cundari, Maurizio Cundari, Maurizio Cundari, Susanna Vestberg, Peik Gustafsson, Sorina Gorcenco, Anders Rasmussen   +6 more
doaj   +1 more source

Frequency-dependent modulation of cerebellar excitability during the application of non-invasive alternating current stimulation

Brain Stimulation, 2021
Background: it is well-known that the cerebellum is critical for the integrity of motor and cognitive actions. Applying non-invasive brain stimulation techniques over this region results in neurophysiological and behavioural changes, which have been ...
Danny Spampinato, Esin Avci, John Rothwell, Lorenzo Rocchi   +3 more
doaj   +1 more source

New roles for the cerebellum in health and disease

Frontiers in Systems Neuroscience, 2013
The cerebellum has a well-established role in maintaining motor coordination and studies of cerebellar learning suggest that it does this by recognizing neural patterns, which it uses to predict optimal movements. Serious damage to the cerebellum impairs
Stacey L Reeber, Tom S. Otis, Roy Vincent Sillitoe   +2 more
doaj   +1 more source

Cerebellar dysfunction in rodent models with dystonia, tremor, and ataxia

Dystonia, 2023
Dystonia is a movement disorder characterized by involuntary co- or over-contractions of the muscles, which results in abnormal postures and movements. These symptoms arise from the pathophysiology of a brain-wide dystonia network.
Meike E. van der Heijden, Meike E. van der Heijden, Roy V. Sillitoe, Roy V. Sillitoe, Roy V. Sillitoe, Roy V. Sillitoe, Roy V. Sillitoe   +6 more
doaj   +1 more source

Multifaceted and Age-Dependent Phenotypes Associated With Biallelic PNPLA6 Gene Variants: Eight Novel Cases and Review of the Literature

Frontiers in Neurology, 2022
A wide spectrum of neurodegenerative diseases has been associated with pathogenic variants in the PNPLA6 (patatin-like phospholipase domain-containing protein 6) gene, including spastic paraplegia type 39, Gordon—Holmes, Boucher—Neuhauser, Oliver—Mc ...
Lorenzo Nanetti, Daniela Di Bella, Stefania Magri, Mario Fichera, Elisa Sarto, Anna Castaldo, Alessia Mongelli, Silvia Baratta, Silvia Fenu, Marco Moscatelli, Maria Teresa Bonati, Andrea Martinuzzi, Caterina Mariotti, Franco Taroni   +13 more
doaj   +1 more source